| Health / Medical Topics |
Monosomy 13q Syndrome
A rare syndrome that is characterized by the partial deletion of the long arm of chromosome 13. Signs and symptoms include low birth weight, craniofacial malformations, hands and feet malformations, and mental and psychomotor retardation. (NCI Thesaurus)
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A chromosomal abnormality consisting of the absence of a copy (homolog) of chromosome 13.
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